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FDA clears Luminex's ARIES C. diff assay

Published 07/24/2017, 11:01 AM
© Reuters.  FDA clears Luminex's ARIES C. diff assay
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  • The FDA grants 510(k) clearance for Luminex's (LMNX -0.2%) ARIES C. difficile Assay which detects both toxin A and toxin B. The ARIES system is an automated benchtop analyzer that generates results in less than two hours.
  • The C. diff assay is the latest addition to the company's gastroenterological diagnostic lineup that includes a GI Pathogen Panel, Enteric Pathogens Test and Norovirus Assay.
  • Now read: Updates To Insulet Thesis: Innovation And Growth Continue


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